Variant report

Variant	rs73044610
Chromosome Location	chr12:10841991-10841992
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs10845205	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832329	chr12:10677094-10845946	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
2	nsv1050613	chr12:10809805-10844399	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10834600-10853800	Weak transcription	Pancreas	Pancrea
2	chr12:10834800-10848600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:10836800-10851200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr12:10838600-10843600	Weak transcription	HSMMtube	muscle
5	chr12:10839800-10849800	Weak transcription	A549	lung
6	chr12:10840000-10848000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:10840600-10848000	Weak transcription	Psoas Muscle	Psoas
8	chr12:10840600-10848600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr12:10840800-10847400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr12:10840800-10848000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr12:10840800-10848000	Weak transcription	Left Ventricle	heart
12	chr12:10841400-10847400	Weak transcription	HSMM	muscle
13	chr12:10841800-10842600	Weak transcription	Aorta	Aorta
14	chr12:10841800-10842800	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr12:10841800-10846400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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